Product Details

SNP ID

rs191916635

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:52582218 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATTTTGTAGATACCTCTTCCAAATG[C/T]ATGATGAAGATGTTCTCATCAACAG

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

ZNF701 PubMed Links

Additional Information

For this assay, SNP(s) [rs12975229] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

ZNF701

Gene Name

zinc finger protein 701

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001172655.1	288	Silent Mutation	TGC,TGT	C119C	NP_001166126.1
NM_018260.2	288	Silent Mutation	TGC,TGT	C53C	NP_060730.2
XM_011527092.1	288	Intron			XP_011525394.1

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